Cyclophosphamide in steroid refractory unclassifiable idiopathic interstitial pneumonia and interstitial pneumonia with autoimmune features (IPAF)

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Idiopathic Interstitial Pneumonia

Division of Pulmonary and Critical Care Medicine and Department of Radiology, University of Michigan Health System, and Department of Biostatistics, University of Michigan School of Public Health, Ann Arbor, Michigan; University of California, San Francisco, San Francisco, California; University of Washington, Seattle, Washington; Mayo Clinic, Scottsdale, Arizona; and Armed Forces Institute of ...

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Characterisation of patients with interstitial pneumonia with autoimmune features.

Patients with interstitial lung disease (ILD) may have features of connective tissue disease (CTD), but lack findings diagnostic of a specific CTD. A recent European Respiratory Society/American Thoracic Society research statement proposed criteria for patients with interstitial pneumonia with autoimmune features (IPAF).We applied IPAF criteria to patients with idiopathic interstitial pneumonia...

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Interstitial pneumonitis with autoimmune features (IPAF): a work in progress.

In clinical practice, it is common to encounter patients with an “idiopathic” interstitial pneumonia (IIP) associated with features suggestive of, but not diagnostic for, a classical connective tissue disease (CTD). In some cases, serological abnormalities are absent and in other cases, serological findings are suggestive of a specific CTD, but systemic clinical features are not. Alternatively,...

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Spontaneous Improvement of Interstitial Pneumonia with Autoimmune Features

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ژورنال

عنوان ژورنال: European Respiratory Journal

سال: 2018

ISSN: 0903-1936,1399-3003

DOI: 10.1183/13993003.02519-2017